Lanes R, Palacios A, Avendano E, Moncada G, Chique G
Department of Endocrinology, Hospital Militar Dr. Carlos Arvelo, Caracas, Venezuela.
Fertil Steril. 1989 Jul;52(1):55-9. doi: 10.1016/s0015-0282(16)60788-4.
To evaluate the effectiveness of intravenous metoclopramide, alone or in combination with luteinizing hormone-releasing hormone (LH-RH), in distinguishing between constitutional delay of puberty and hypogonadotropic hypogonadism, 12 patients with constitutional delay of puberty and 10 patients with hypogonadotropic hypogonadism were studied. All patients received 10 mg/m2 of intravenous metoclopramide and 100 micrograms of intravenous LH-RH on separate days. The mean prolactin (PRL) response following metoclopramide was significantly higher in the constitutional delay of puberty group when compared with the hypogonadotropic hypogonadism patients (P less than 0.01 at 15, 30, 45, and 60 minutes); all patients with constitutional delay of puberty increased their PRL level to greater than or equal to 60 ng/ml, except one who had a peak PRL level of 38 ng/ml. While only 2 of the hypogonadotropic hypogonadism subjects reached a peak PRL concentration of greater than or equal to 60 ng/ml, 4 had peak PRL levels greater than 38 ng/ml. The mean LH and follicle-stimulating hormone (FSH) responses after LH-RH were significantly higher in the constitutional delay of puberty group (P less than 0.01 at 30, 45, and 60 minutes for LH and P less than 0.01 at 45 and 60 minutes for FSH). All constitutional delay of puberty subjects responded to both the metoclopramide and LH-RH tests, while patients with hypogonadotropic hypogonadism responded only to one or to neither of these tests. Therefore, while metoclopramide alone did not allow us to clearly distinguish constitutional delay of puberty from hypogonadotropic hypogonadism, the combined use of both of these stimuli permitted us to detect all subjects with constitutional delay of puberty.
为评估静脉注射胃复安单独使用或与促黄体生成素释放激素(LH-RH)联合使用,在区分体质性青春期延迟和低促性腺激素性性腺功能减退方面的有效性,对12例体质性青春期延迟患者和10例低促性腺激素性性腺功能减退患者进行了研究。所有患者在不同日期分别接受10mg/m²的静脉注射胃复安和100μg的静脉注射LH-RH。与低促性腺激素性性腺功能减退患者相比,体质性青春期延迟组在注射胃复安后催乳素(PRL)的平均反应在15、30、45和60分钟时显著更高(P<0.01);除1例PRL峰值水平为38ng/ml的患者外,所有体质性青春期延迟患者的PRL水平均升高至≥60ng/ml。而低促性腺激素性性腺功能减退患者中只有2例PRL峰值浓度≥60ng/ml,4例PRL峰值水平>38ng/ml。LH-RH注射后,体质性青春期延迟组促黄体生成素(LH)和促卵泡生成素(FSH)的平均反应显著更高(LH在30、45和60分钟时P<0.01,FSH在45和60分钟时P<0.01)。所有体质性青春期延迟受试者对胃复安和LH-RH试验均有反应,而低促性腺激素性性腺功能减退患者仅对其中一项试验有反应或对两项试验均无反应。因此,虽然单独使用胃复安无法使我们明确区分体质性青春期延迟和低促性腺激素性性腺功能减退,但这两种刺激联合使用使我们能够检测出所有体质性青春期延迟的受试者。